G38A (p.Gly38Ala) variant of KCNB1 (Q14721)
G38A (p.Gly38Ala) in KCNB1 (Q14721) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided.
G38A (p.Gly38Ala) variant details
- p.Gly38Ala
- rs1555801618
- ClinGen CA408951839
- ClinVar RCV000498592
- Ensembl rs1555801618
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance